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rs777524402

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs777524402(C;G)
Make rs777524402(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11110731
GeneLDLR
is asnp
is mentioned by
dbSNPrs777524402
ebirs777524402
HLIrs777524402
Exacrs777524402
Varsomers777524402
Maprs777524402
PheGenIrs777524402
hapmaprs777524402
1000 genomesrs777524402
hgdprs777524402
ensemblrs777524402
gopubmedrs777524402
geneviewrs777524402
scholarrs777524402
googlers777524402
pharmgkbrs777524402
gwascentralrs777524402
openSNPrs777524402
23andMers777524402
23andMe allrs777524402
SNP Nexus

SNPshotrs777524402
SNPdbers777524402
MSV3drs777524402
GWAS Ctlgrs777524402
Max Magnitude0
ClinVar
Risk rs777524402(G;G)
Alt rs777524402(G;G)
Reference rs777524402(C;C)
Significance Probable-Pathogenic
Disease Familial hypercholesterolemia
Variation info
Gene LDLR
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000019.9:g.11221407C>G
CLNSRC LDLR @ LOVD
CLNACC RCV000238375.1,